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Volumn 48, Issue 31, 2007, Pages 5435-5438

A new strategy for the synthesis of optically active benzylic fluorides and corresponding five-membered heteroaromatic analogues

Author keywords

[No Author keywords available]

Indexed keywords

BENZYL DERIVATIVE; FLUORIDE; HETEROCYCLIC COMPOUND;

EID: 34347326071     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.06.007     Document Type: Article
Times cited : (27)

References (27)
  • 3
    • 0003536898 scopus 로고
    • Banks R.E., Smart B.E., and Tatlow J.C. (Eds), Plenum, New York and references cited therein
    • In: Banks R.E., Smart B.E., and Tatlow J.C. (Eds). Organofluorine Chemistry: Principles and Commercial Applications (1994), Plenum, New York and references cited therein
    • (1994) Organofluorine Chemistry: Principles and Commercial Applications
  • 4
    • 34347352352 scopus 로고    scopus 로고
    • Ojima, I.; McCarthy, J. R.; Welch, J. T. Biomedical Frontiers in Fluorine Chemistry, ACS Symposium Series 639. ACS: Washington, DC, 1996.
  • 6
    • 0023237559 scopus 로고
    • and references cited therein
    • Welch J.T. Tetrahedron 43 (1987) 3123 and references cited therein
    • (1987) Tetrahedron , vol.43 , pp. 3123
    • Welch, J.T.1
  • 7
    • 34347364836 scopus 로고    scopus 로고
    • Sai Krishna Murthy, A.; Tardivel, R.; Grée, R. Product Subclass 6: Benzylic Fluorides, Science of Synthesis. Georg Thieme Verlag, 2006; p 295.
  • 8
    • 54249104638 scopus 로고    scopus 로고
    • Asymmetric Synthesis of Monofluorinated Compounds having the Fluorine Atom Vicinal to π-Systems
    • Soloshonok V.A. (Ed), ACS Publications Division and Oxford University Press, Washington, DC
    • Prakesch M., Grée D., and Grée R. Asymmetric Synthesis of Monofluorinated Compounds having the Fluorine Atom Vicinal to π-Systems. In: Soloshonok V.A. (Ed). Fluorine Containing Synthons (2005), ACS Publications Division and Oxford University Press, Washington, DC 173
    • (2005) Fluorine Containing Synthons , pp. 173
    • Prakesch, M.1    Grée, D.2    Grée, R.3
  • 12
    • 11144341001 scopus 로고    scopus 로고
    • For recent reviews on asymmetric fluorinations, including electrophilic fluorinations, see:
    • For recent reviews on asymmetric fluorinations, including electrophilic fluorinations, see:. Ma J.-A., and Cahard D. Chem. Rev. 104 (2004) 6119
    • (2004) Chem. Rev. , vol.104 , pp. 6119
    • Ma, J.-A.1    Cahard, D.2
  • 22
    • 34347333698 scopus 로고    scopus 로고
    • note
    • 3) -172.18 (the signal for the other diastereoisomer is at -172.16).
  • 25
    • 34347353470 scopus 로고    scopus 로고
    • note
    • 3).
  • 27
    • 34347338921 scopus 로고    scopus 로고
    • note
    • 3) -177.98 (dqq, J = 46.6, J = 23.4, J = 1.6).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.